510(k) K882751 ยท EJK Liner, Cavity, Calcium Hydroxide
GLASS IONOMER BASE
| Applicant | Dentsply Intl., York PA, US |
| Decision | Substantially Equivalent, Nov 29, 1988 |
| Received | Jul 5, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882751
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.